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Summary

Isoform:
Position:
557
Ref:
T
Mutation:
A
PTM impact:
proximal
PTM affected:
1
Kinases:

Clinical Information

Cancer types: (TCGA MC3)

PAAD

Cancer types: (PCAWG)

no data

Disease Annotations: (ClinVar)

no data

Minor Allele Frequency: (ESP6500)

no data

Minor Allele Frequency: (1000 Genomes)

no data

PTM Site: 558K

Affected site:

Position: 558
Residue: K
Type: ubiquitination

Impact:

proximal

Other known mutations affecting this site

Mutation In sequence Distance Impact
564S VVSSDPTKTAARD[I/S]II 6
distal
563G VVSSDPTKTAAR[D/G]DII 5
distal
561S VVSSDPTKTA[A/S]ARDII 3
distal
557A VVSSDP[T/A]TKTAARDII 1
proximal

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